Label: MARQUIS GEL FORMULA gel

  • NDC Code(s): 76585-009-11, 76585-009-12, 76585-009-13, 76585-009-14, view more
    76585-009-15, 76585-009-17, 76585-009-18
  • Packager: Marquis XT LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 29, 2024

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  • Active Ingredient(s)

    Alcohol 70% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
    • in eyes
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    glycerin, purified water USP, acrylates, copolymer, aloe barbadensis (aloe vera) leaf juice, fragrance, isopropyl myristste, propylene glycol, trilsopropanolamine

  • Package Label - Principal Display Panel

    Gel 008

  • INGREDIENTS AND APPEARANCE
    MARQUIS GEL FORMULA 
    marquis gel formula gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76585-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.005 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) 1 mL  in 100 mL
    DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) 0.00035 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76585-009-173785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    2NDC:76585-009-11473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    3NDC:76585-009-13236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    4NDC:76585-009-14946 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    5NDC:76585-009-1512113 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    6NDC:76585-009-121040875 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    7NDC:76585-009-18355 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/2020
    Labeler - Marquis XT LLC (117496233)
    Establishment
    NameAddressID/FEIBusiness Operations
    Marquis XT LLC117496233manufacture(76585-009)
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